Rare-earth doped gain fibers

ABSTRACT

Rare earth oxides doped multicomponent glass fibers for laser generation and amplification, including a core and a cladding, the core comprising at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K 2 O, Na 2 O, Li 2 O, Y 2 O 3 , or combinations; wherein the mode of the core is guided with step index difference between the core and the cladding, a numerical aperture of the fiber is between 0.01 and 0.04; core diameter is from 25 to 120 micron, and a length of the gain fiber is shorter than 60 cm.

FIELD OF THE INVENTION

This invention relates to rare-earth doped gain fibers.

BACKGROUND OF THE INVENTION

High-power, pulsed fiber lasers are of great interest in applications such as laser micromachining, material processing, nonlinear optics, and laser sensing. Prior art high power fiber lasers are commonly achieved via the means of making a fiber-based master-oscillator-power-amplifier (MOPA).

SUMMARY OF THE INVENTION

A Ytterbium doped multicomponent glass fiber for laser generation and amplification from about 1.01 to about 1.12 micron wavelength is disclosed. Applicants' Ytterbium doped multicomponent glass fiber comprises a core and a cladding.

The core glass of Applicants' Ytterbium doped multicomponent glass fiber contains at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations and ytterbium oxides from about 3 to about 50 weight percent. The mode of the core is guided with step index difference between the core and the cladding, and the numerical aperture of the fiber is between about 0.01 and about 0.04. The core diameter is from about 25 to about 60 micron. The length of the gain fiber is shorter than 60 cm.

An Erbium doped multicomponent glass fiber for laser generation and amplification from 1.51 to 1.65 micron wavelength is disclosed. Applicants' Erbium doped multicomponent glass fiber comprises a core and a cladding.

The core glass of the fiber contains at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations and ytterbium oxide from about 0.5 to about 20 weight percent. The mode of the core is guided with step index difference between the core and the cladding, and the numerical aperture of the fiber is between about 0.01 and about 0.04. The core diameter is from about 30 to about 90 microns. The length of the gain fiber is shorter than 60 cm.

A Thulium doped multicomponent glass fiber for laser generation and amplification from 1.75 to 2.05 micron wavelength is disclosed. Applicants' Thulium doped multicomponent glass fiber comprises a core and a cladding.

The core glass of the fiber contains at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations and ytterbium oxide from about 2 to about 30 weight percent. The mode of the core is guided with step index difference between the core and the cladding, and the numerical aperture of the fiber is between about 0.01 and about 0.04. The core diameter is from about 35 to about 120 micron. The length of the gain fiber is shorter than 60 cm.

A Holmium doped multicomponent glass fiber for laser generation and amplification from 1.98 to 2.2 micron wavelength is disclosed. Applicants' Holmium doped multicomponent glass fiber comprises a core and a cladding.

The core glass of the fiber contains at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations and ytterbium oxide from about 0.5 to about 20 weight percent. The mode of the core is guided with step index difference between the core and the cladding, and the numerical aperture of the fiber is between about 0.01 and about 0.04. The core diameter is from about 35 to about 120 microns. The length of the gain fiber is shorter than 60 cm.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be better understood from a reading of the following detailed description taken in conjunction with the drawings in which like reference designators are used to designate like elements, and in which:

FIG. 1 illustrates a schematic of a prior art fiber-based master-oscillator-power-amplifier (MOPA);

FIG. 2 illustrates a cross section view of Applicants' rare-earth doped fiber;

FIG. 3 illustrates a cross section view of Applicants' double cladding rare-earth doped fiber; and

FIG. 4 illustrates a cross section view of Applicants' polarization maintaining double cladding rare-earth doped fiber.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

This invention is described in preferred embodiments in the following description with reference to the Figures, in which like numbers represent the same or similar elements. Reference throughout this specification to “one embodiment,” “an embodiment,” or similar language means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, appearances of the phrases “in one embodiment,” “in an embodiment,” and similar language throughout this specification may, but do not necessarily, all refer to the same embodiment.

The described features, structures, or characteristics of the invention may be combined in any suitable manner in one or more embodiments. In the following description, numerous specific details are recited to provide a thorough understanding of embodiments of the invention. One skilled in the relevant art will recognize, however, that the invention may be practiced without one or more of the specific details, or with other methods, components, materials, and so forth. In other instances, well-known structures, materials, or operations are not shown or described in detail to avoid obscuring aspects of the invention.

High-power, pulsed fiber lasers are of great interest in applications such as laser micromachining, material processing, nonlinear optics, and laser sensing. High power fiber lasers are commonly achieved via the means of making a fiber-based master-oscillator-power-amplifier (MOPA).

FIG. 1 illustrates the schematic of MOPA configuration. The seed laser is amplified by a fiber amplifier. Typically the seed laser is amplified by a rare-earth doped gain fiber, which is energized by pump laser.

FIG. 2 shows the cross section view of a rare-earth doped fiber. The pump laser is combined together with seed laser via the so-called signal and pump combiner. The amplified seed laser can be amplified again in order to achieve higher pulse energy and higher peak power. When more than one amplifier is used, the fiber amplifiers are called multi-stage amplifiers. In order to achieve high power, double-cladding rare-earth doped gain fiber is typically used.

FIG. 3 illustrate the typically cross section view of double cladding gain fiber. The core is used to guide the signal. Here it is called seed laser. The inner cladding is used to confine the pump lasers. The core is typically rare-earth doped glass. The rare-earth ion produces gain. For example, ytterbium ion (Yb³⁺) and neodymium (Nd³⁺) offer gain near 1 micron wavelength, erbium ion (Er³⁺) produces gain near 1.55 micron, thulium ion (Tm³⁺) and holmium ion (Ho³⁺) can produce gain near 2 micron wavelength.

The inner cladding is typically undoped glass material with a lower refractive index in order to form waveguide in the core. The external cladding layer can be glass material or polymer material, which has a lower refractive index to confine the pump laser in the inner cladding. In order to generate polarization maintaining (PM) output, PM gain fiber is needed.

FIG. 4 illustrates the cross section view of typical PM fiber.

High pulse energy and high peak power is needed for many applications. Due to the strong transverse confinement and long interaction length, power scaling of fiber amplifier is limited by the onset of nonlinear effects.

For single-frequency/narrow-band amplifiers, stimulated Brillouin scattering (SBS) has the lowest threshold and possibly causes much of the signal light to be reflected back. For broader signal bandwidth, stimulated Raman scattering (SRS) can happen at higher power levels and transfer a lot of signal power into unwanted new wavelength components.

The SBS threshold power for narrow band signal is determined by the following equation 1:

$\begin{matrix} {P_{B\; 0} = \frac{21{bA}_{e}}{g_{B}L_{e}}} & (1) \end{matrix}$

Where b is a number between 1 and 2 which depends on polarization state. A_(e) is the effective area. gB is the SBS gain coefficient. Le is the effective transmission length of the fiber.

The threshold power for SRS can be described as the following equation (2)

$\begin{matrix} {P_{R0} = \frac{16A_{e}}{g_{R}L_{e}}} & (2) \end{matrix}$

wherein gR is the SRS gain coefficient.

Therefore, the threshold of optical nonlinearity in fiber increases with the effective area and decreases with the effective transmission length of the fiber. The effective area increase with the core diameter of the fiber and the mode filed diameter of the fiber. For single mode core, the mode field diameter is typically proportional to the physical core diameter of the fiber. In order to increase the pulse energy and peak power of the fiber laser one need to increase the threshold of the optical nonlinearity of gain fiber. In order to increase the threshold of the optical nonlinearity of gain fiber, the length of the gain fiber should be short and the core diameter of the gain fiber should be large.

The length of the gain fiber is limited by pump absorption. Cladding pumped fiber amplifiers often have a length of many meters for efficiently absorbing of pump light. A high doping concentration can improve the absorption and then shorten the length of the gain fiber. However, the doping concentration of typical silica fiber is limited. So typically a few meter long gain fiber is used.

The core diameter is limited in order to ensure the fiber is single mode fiber. The beam quality will degrade and is no longer single mode when the V number of the fiber is more than 2,405,

$\begin{matrix} {V = {\frac{2\pi}{\lambda}{aNA}}} & (3) \end{matrix}$

where λ is the vacuum wavelength, a is the radius of the fiber core, and NA is the numerical aperture. As can be seen in the equation (3), a lower NA value can compensate the increased core size and keep the V number as low as possible.

However there is also a limit to reduce the NA for conventional step index fiber. U.S. Pat. No. 8,774,590 disclosed a refractive index difference between the core the clad of 0.05 to 0.30% of silica fiber. This patent teaches that a light storing effect of the optical fibers cannot be sufficiently obtained when the relative refractive index difference between the core and clad is lower than 0.05%. The refractive index of silica glass is approximately 1.45. The refractive index of the core glass is 1.4507. So the NA of the fiber should be near 0.04 by using the following equation 4:

NA=√n _(core) ² −n _(clad) ²  (4)

Nclad=1.45 Ncore=1.45*(1+0.0005)=1.4507

Therefore NA=0.046

When the NA is 0.046, the single mode core diameters are 16.65 micron for 1 micron wavelength laser, 25.8 micron for 1.55 micron wavelength laser, and 33.3 micron for 2 micron wavelength laser in according to equation (3). Although U.S. Pat. No. 8,774,590 claims a core diameter of 20 to 30 micron for ytterbium doped fiber laser (ytterbium doped fiber laser wavelength is 1 micron), the V number is already larger than 2.405, which means it is not truly single mode fiber anymore. Fiber bending is needed in order to filter out the higher order mode. So the true single mode core diameter near 1 micron is approximately 16.65 micron.

Further, silica fibers for U.S. Pat. No. 8,774,590 are formed using MCVD (Modified Chemical Vapor Deposition) or VAD (Vapor Axial Deposition) method to deposit the core material. A problem, however, arises with these conventional optical fibers in that current optical fiber manufacturing methods are restricted in their ability to precisely control the indices of refraction of the core material (n_(core)) and the cladding material (n_(clad)). Because of this restricted ability, in commercially practical fiber, the difference between n_(core) and n_(clad) is usually limited by design to no less than 0.1%. This, in turn, restricts the designed size of the core diameter for a given wavelength, and/or restricts the wavelengths of single-mode operation of a fiber for a given core diameter.

For example, one common optical fiber manufacturing method referred to as flame hydrolysis uses a burner to fire a combination of metal halide particles and SiO₂ (called a “soot”) onto a rotating graphite or ceramic mandrel to make the optical fiber perform. See Keiser, Optical Fiber Communications, 2nd ed., McGraw-Hill (1991), which is incorporated by reference herein, at pp. 63-68.

The index of refraction is controlled by controlling the constituents of the metal halide vapor stream during the deposition process. The process is “open loop” without a feedback mechanism to precisely control the ultimate index of refraction of the optical material. Moreover, the metal halide vapor stream is limited in its controllability and in its ability to control the ultimate index of refraction of the optical material.

During the process a good portion of the material will be vaporized, therefore, it is extremely difficult to control the difference of the refractive index difference to close to 0.05% (equals to NA of 0.046). So most gain fibers have NA of 0.08 or larger.

Another approach is to use the so-called photonic crystal fiber (PCF) design to achieve a large core diameter. A photonic crystal fiber (also called holey fiber, hole-assisted fiber, microstructure fiber, or microstructured fiber) is an optical fiber which obtains its waveguide properties not from a spatially varying glass composition but from an arrangement of very tiny and closely spaced air holes which go through the whole length of fiber. Such air holes can be obtained by using a preform with holes, made e.g. by stacking capillary and/or solid tubes and inserting them into a larger tube. These fibers are not step index fibers and their guiding mechanism is different from step index fibers.

Laser-active PCFs for fiber lasers and amplifiers can be fabricated, e.g., by using a rare-earth-doped rod as the central element of the preform assembly. Rare earth dopants (e.g. ytterbium or erbium) tend to increase the refractive index, the guiding properties are determined by the photonic microstructure only and not by a conventional-type refractive index difference. For high-power fiber lasers and amplifiers, double-clad PCFs can be used, where the pump cladding is surrounded by an air cladding region (air-clad fiber). Due to the very large contrast of refractive index, the pump cladding can have a very high numerical aperture (NA), which significantly lowers the requirements on the pump source with respect to beam quality and brightness.

Such PCF designs can also have very large mode areas of the fiber core while guiding only a single mode for diffraction-limited output, and are thus suitable for very high output powers with excellent beam quality.

But PCF (microstructured fiber) has many disadvantages including difficulty for fabrication, difficulty for fusion splicing, poor thermal conductivity of the air-gap, and relatively low doping in the core of the fiber. Therefore, it is strongly desired to have a step index fiber with a large core diameter, which is truly single mode fiber.

We disclose a type of gain fiber, which has a numerical aperture of between 0.01 and 0.04, resulting an extremely large single mode core diameter. Here the host of the rare-earth ions, the gain elements, is the multicomponent glasses, which is different from the most commonly used silica glass.

It is well known that silica fibers are made with vapor deposition method, which contains almost no alkali metal ions nor alkaline earth metal ions because these ions are not compatible with vapor deposition process. The total content should be less than 0.1 weight percent. Multicomponent glasses always contain alkali metal ions or alkaline earth metal ions, which is at least more than 1 weight percent.

The alkali metals include Lithium (Li), Sodium (Na), Potassium (K), and the alkaline earth metals are beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), and barium (Ba). These alkali metal ions or alkaline earth metal ions are called glass network modifier in multicomponent glasses. Other metal ions such as Zn and Pb can act as glass network modifiers, which again is not compatible with vapor deposit process.

Multicomponent glasses include phosphate glasses, silicate glasses, tellurite glasses, germanate glasses, et al. U.S. Pat. No. 6,816,514, in the name of Jiang disclose rare-earth doped phosphate-glass fiber for fiber laser application. U.S. Pat. No. 6,859,606 in the name of Jiang, disclose erbium doped boro-tellurite glasses for 1.5 micron fiber amplification. U.S. Pat. No. 7,298,768 in the name of Jiang, disclose germanate glasses for fiber lasers. U.S. Pat. No. 8,121,154 to Jiang disclosed silicate glasses for fiber laser applications. Multicomponent glass fibers are used for fiber laser application because of theirs capability of high doping concentrations. These patents limit their advantages of using a relatively shorter piece of gain fiber compared to silica glass fiber.

But for high pulse energy fiber lasers, a large core diameter is critical. Applicants have discovered that a large core diameter can be obtained from multicomponent glass gain fibers. The numerical aperture can be from 0.01 to 0.04. Therefore, the core diameter can be from 25 micron to 60 micron for 1 micron wavelength, 35 micron to 90 micron for 1.55 micron wavelength, and 45 micron to 120 micron for 2 micron wavelength.

Applicants dope high rare-earth ions into the fiber, so the total length of the gain fiber is not longer than 60 cm. Therefore the gain fiber can be packaged straight. No bending is necessary.

Because of the extremely large core diameter and relatively short length of gain fiber, a peak power of greater than 50 kW can be achieved without optical nonlinearity.

Applicants have developed a new cladding pumped polarization maintaining Yb doped fiber based on silicate materials. With large mode size, high Yb doping level and low NA, the fiber amplifier has achieved record high threshold for nonlinear effects while keep excellent diffraction limited beam quality. Table 1 compares the parameters of Applicants' Yb-doped fiber with most popular commercial cladding pumped Yb fibers.

TABLE 1 Fiber Commercial Commercial Yb1200- Applicants' Yb1200-10/125 20/125 Yb #35 Core diameter 10 μm 20 μm 30 μm Estimated mode area 80 μm² 320 μm² 720 μm² A_(e) NA 0.08 0.08  0.025 V number @1064 nm 2.36 4.74 2.21 Fiber modes Single mode Multimode Single mode Inner cladding 125 μm 125 μm 135 μm diameter Doping concentration 1.2 weight percent 1.2 weight 10 weight percent percent Nominal cladding ~7 dB/m ~30 dB/m ~500 dB/m absorption at 976 nm (For small signal) Fiber length for 7.1 m 1.7 m 0.1 m nominal 50 dB absorption at 976 nm Nonlinear threshold P₀ 16P₀ 640P₀

As shown in Table 1, Applicants' fiber Yb#35 has an estimated nonlinear threshold power ˜640 times higher than that of the commercial fiber.

TABLE 2 compares the SBS /SRS thresholds for different input signals between Applicants' fiber and commercial fibers. The nonlinear threshold of Applicants' fiber is many times higher than commercial fibers. The threshold of Applicants' fiber is always many times higher than the typical commercial fiber, which means high pulse energy can be achieved.

TABLE 2 Fiber Amplifier Commercial Commercial Applicants' Yb1200-10/125 Yb1200-20/125 Yb #35 7.1 m 1.7 m 0.1 m SBS threshold for 5.9 W 94 W 3.7 kW narrow band CW signal SRS threshold for 2.8 kW 45 kW 1.8 MW CW signal SRS threshold 280 μJ 4.5 mJ 180 mJ energy for 100 ns pulse SRS threshold 28 μJ 450 μJ 18 mJ energy for 10 ns pulse SRS threshold 2.8 μJ 45 μJ 1.8 mJ energy for 1 ns pulse

While the preferred embodiments of the present invention have been illustrated in detail, it should be apparent that modifications and adaptations to those embodiments may occur to one skilled in the art without departing from the scope of the present invention. 

We claim:
 1. A Ytterbium doped multicomponent glass fiber for laser generation and amplification from 1.01 to 1.12 micron wavelength, comprising: a core; and a cladding; wherein said core comprises: at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations; and ytterbium oxide at a level from about 3 to about 50 weight percent; wherein: the mode of the core is guided with step index difference between the core and the cladding; a numerical aperture of the fiber is between 0.01 and 0.04; core diameter is from 25 to 60 micron; and a length of the gain fiber is shorter than 60 cm.
 2. The Ytterbium doped multicomponent glass fiber of claim 1, wherein said ytterbium oxide is present at a level from about 5 to about 25 weight percent.
 3. The Ytterbium doped multicomponent glass fiber of claim 1, wherein a core diameter is from about 30 microns to about 50 microns.
 4. The Ytterbium doped multicomponent glass fiber of claim 1, wherein a fiber length is from about 5 cm to about 45 cm.
 5. The Ytterbium doped multicomponent glass fiber of claim 1, wherein the fiber can be polarization maintain fiber.
 6. An Erbium doped multicomponent glass fiber for laser generation and amplification from 1.51 to 1.65 micron wavelength, comprising: a core; a cladding; wherein: said core comprises at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations; and erbium oxide at a level from about 0.5 to about 20 weight percent; wherein: a mode of the core is guided with step index difference between the core and the cladding; the numerical aperture of the fiber is between 0.01 and 0.04; the core diameter is from about 30 microns to about 90 microns; a length of the gain fiber is shorter than 60 cm.
 7. The Erbium doped multicomponent glass fiber of claim 6, wherein said erbium oxide is present at a level from about 1 to about 5 weight percent.
 8. The Erbium doped multicomponent glass fiber of claim 6, wherein a core diameter is from about 35 microns to about 60 microns.
 9. The Erbium doped multicomponent glass fiber of claim 6, wherein a fiber length is from about 4 cm to about 45 cm.
 10. The Erbium doped multicomponent glass fiber of claim 6, wherein the fiber can be polarization maintain fiber.
 11. A Thulium doped multicomponent glass fiber for laser generation and amplification from 1.75 to 2.05 micron wavelength comprising: a core; a cladding; wherein said core of the fiber comprises at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations thereof; and thulium oxide at a level from about 2 weight percent to about 30 weight percent; wherein a mode of the core is guided with step index difference between the core and the cladding; a numerical aperture of the fiber is between about 0.01 and about 0.04; a core diameter is from about 35 to 120 micron; a length of the gain fiber is shorter than 60 cm.
 12. The Thulium doped multicomponent glass fiber of claim 11, wherein said thulium oxide is present at a level from about 1 to about 5 weight percent.
 13. The Thulium doped multicomponent glass fiber of claim 11, wherein a core diameter is from about 35 microns to about 60 microns.
 14. The Thulium doped multicomponent glass fiber of claim 11, wherein a fiber length is from about 4 cm to about 45 cm.
 15. The Thulium doped multicomponent glass fiber of claim 11, wherein the fiber can be polarization maintain fiber.
 16. A Holmium doped multicomponent glass fiber for laser generation and amplification from 1.98 to 2.2 micron wavelength, comprising: a core; a cladding; wherein: said core glass of the fiber contains at least 2 weight percent glass network modifier selected from BaO, CaO, MgO, ZnO, PbO, K₂O, Na₂O, Li₂O, Y₂O₃, or combinations thereof; holmium oxide at a level from about 0.5 to about 20 weight percent; a mode of the core is guided with step index difference between the core and the cladding; a numerical aperture of the fiber is between about 0.01 and about 0.04; a core diameter is from about 35 to about 120 micron; a length of said gain fiber is shorter than 60 cm.
 17. The Holmium doped multicomponent glass fiber of claim 16, wherein said holmium oxide is present at a level from about 1 to about 5 weight percent.
 18. The Holmium doped multicomponent glass fiber of claim 16, wherein a core diameter is from about 40 microns to about 90 microns.
 19. The Holmium doped multicomponent glass fiber of claim 16, wherein a fiber length is from about 5 cm to about 45 cm.
 20. The Holmium doped multicomponent glass fiber of claim 16, wherein the fiber can be polarization maintain fiber. 